Vimpat

Country: European Union

Language: English

Source: EMA (European Medicines Agency)

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Active ingredient:

lacosamide

Available from:

UCB Pharma SA

ATC code:

N03AX18

INN (International Name):

lacosamide

Therapeutic group:

Antiepileptics,

Therapeutic area:

Epilepsy

Therapeutic indications:

Vimpat is indicated as monotherapy and adjunctive therapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy.

Product summary:

Revision: 46

Authorization status:

Authorised

Authorization date:

2008-08-29

Patient Information leaflet

                                134
B. PACKAGE LEAFLET
135
PACKAGE LEAFLET: INFORMATION FOR THE PATIENT
VIMPAT 50 MG FILM-COATED TABLETS
VIMPAT 100 MG FILM-COATED TABLETS
VIMPAT 150 MG FILM-COATED TABLETS
VIMPAT 200 MG FILM-COATED TABLETS
lacosamide
READ ALL OF THIS LEAFLET CAREFULLY BEFORE YOU START TAKING THIS
MEDICINE BECAUSE IT CONTAINS
IMPORTANT INFORMATION FOR YOU.
•
Keep this leaflet. You may need to read it again.
•
If you have any further questions, ask your doctor or pharmacist.
•
This medicine has been prescribed for you only. Do not pass it on to
others. It may harm them,
even if their signs of illness are the same as yours.
•
If you get any side effects, talk to your doctor or pharmacist. This
includes any possible side
effects not listed in this leaflet. See section 4.
WHAT IS IN THIS LEAFLET
1.
What Vimpat is and what it is used for
2.
What you need to know before you take Vimpat
3.
How to take Vimpat
4.
Possible side effects
5.
How to store Vimpat
6.
Contents of the pack and other information
1.
WHAT VIMPAT IS AND WHAT IT IS USED FOR
WHAT VIMPAT IS
Vimpat contains lacosamide. This belongs to a group of medicines
called “antiepileptic medicines”.
These medicines are used to treat epilepsy.
•
You have been given this medicine to lower the number of fits
(seizures) you have.
WHAT VIMPAT IS USED FOR
•
Vimpat is used:
▪
on its own and in association with other antiepileptic medicines in
adults, adolescents
and children aged 2 years and older to treat a certain type of
epilepsy characterised by
the occurrence of partial-onset seizure with or without secondary
generalisation. In this
type of epilepsy, fits first affect only one side of your brain.
However, these may then
spread to larger areas on both sides of your brain;
▪
in association with other antiepileptic medicines in adults,
adolescents and children
aged 4 years and older to treat primary generalised tonic-clonic
seizures (major fits,
including loss of consciousness) in patients with idiopathic
generalised epilepsy (the
type of epilepsy that is thought to h
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                1
ANNEX I
SUMMARY OF PRODUCT CHARACTERISTICS
2
1.
NAME OF THE MEDICINAL PRODUCT
Vimpat 50 mg film-coated tablets
Vimpat 100 mg film-coated tablets
Vimpat 150 mg film-coated tablets
Vimpat 200 mg film-coated tablets
2.
QUALITATIVE AND QUANTITATIVE COMPOSITION
Vimpat 50 mg film-coated tablets
Each film-coated tablet contains 50 mg lacosamide.
Vimpat 100 mg film-coated tablets
Each film-coated tablet contains 100 mg lacosamide.
Vimpat 150 mg film-coated tablets
Each film-coated tablet contains 150 mg lacosamide.
Vimpat 200 mg film-coated tablets
Each film-coated tablet contains 200 mg lacosamide.
For the full list of excipients, see section 6.1.
3.
PHARMACEUTICAL FORM
Film-coated tablet
Vimpat 50 mg film-coated tablets
Pinkish, oval film-coated tablets with approximate dimensions of 10.4
mm x 4.9 mm, and debossed
with ‘SP’ on one side and ‘50’ on the other side.
Vimpat 100 mg film-coated tablets
Dark yellow, oval film-coated tablets with approximate dimensions of
13.2 mm x 6.1 mm, and
debossed with ‘SP’ on one side and ‘100’ on the other side.
Vimpat 150 mg film-coated tablets
Salmon, oval film-coated tablets with approximate dimensions of 15.1
mm x 7.0 mm, and debossed
with ‘SP’ on one side and ‘150’ on the other side.
Vimpat 200 mg film-coated tablets
Blue, oval film-coated tablets with approximate dimensions of 16.6 mm
x 7.8 mm, and debossed with
‘SP’ on one side and ‘200’ on the other side.
3
4.
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
Vimpat is indicated as monotherapy in the treatment of partial-onset
seizures with or without
secondary generalisation in adults, adolescents and children from 2
years of age with epilepsy.
Vimpat is indicated as adjunctive therapy
•
in the treatment of partial-onset seizures with or without secondary
generalisation in adults,
adolescents and children from 2 years of age with epilepsy.
•
in the treatment of primary generalised tonic-clonic seizures in
adults, adolescents and
children from 4 years of age with idiopathic generalised epilep
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 08-01-2024
Summary of Product characteristics Summary of Product characteristics Bulgarian 08-01-2024
Public Assessment Report Public Assessment Report Bulgarian 25-03-2024
Patient Information leaflet Patient Information leaflet Spanish 08-01-2024
Public Assessment Report Public Assessment Report Spanish 25-03-2024
Patient Information leaflet Patient Information leaflet Czech 08-01-2024
Public Assessment Report Public Assessment Report Czech 25-03-2024
Patient Information leaflet Patient Information leaflet Danish 08-01-2024
Public Assessment Report Public Assessment Report Danish 25-03-2024
Patient Information leaflet Patient Information leaflet German 08-01-2024
Public Assessment Report Public Assessment Report German 25-03-2024
Patient Information leaflet Patient Information leaflet Estonian 08-01-2024
Public Assessment Report Public Assessment Report Estonian 25-03-2024
Patient Information leaflet Patient Information leaflet Greek 08-01-2024
Public Assessment Report Public Assessment Report Greek 25-03-2024
Patient Information leaflet Patient Information leaflet French 08-01-2024
Public Assessment Report Public Assessment Report French 25-03-2024
Patient Information leaflet Patient Information leaflet Italian 08-01-2024
Public Assessment Report Public Assessment Report Italian 25-03-2024
Patient Information leaflet Patient Information leaflet Latvian 08-01-2024
Public Assessment Report Public Assessment Report Latvian 25-03-2024
Patient Information leaflet Patient Information leaflet Lithuanian 08-01-2024
Summary of Product characteristics Summary of Product characteristics Lithuanian 08-01-2024
Public Assessment Report Public Assessment Report Lithuanian 25-03-2024
Patient Information leaflet Patient Information leaflet Hungarian 08-01-2024
Summary of Product characteristics Summary of Product characteristics Hungarian 08-01-2024
Public Assessment Report Public Assessment Report Hungarian 25-03-2024
Patient Information leaflet Patient Information leaflet Maltese 08-01-2024
Public Assessment Report Public Assessment Report Maltese 25-03-2024
Patient Information leaflet Patient Information leaflet Dutch 08-01-2024
Public Assessment Report Public Assessment Report Dutch 25-03-2024
Patient Information leaflet Patient Information leaflet Polish 08-01-2024
Public Assessment Report Public Assessment Report Polish 25-03-2024
Patient Information leaflet Patient Information leaflet Portuguese 08-01-2024
Summary of Product characteristics Summary of Product characteristics Portuguese 08-01-2024
Public Assessment Report Public Assessment Report Portuguese 25-03-2024
Patient Information leaflet Patient Information leaflet Romanian 08-01-2024
Public Assessment Report Public Assessment Report Romanian 25-03-2024
Patient Information leaflet Patient Information leaflet Slovak 08-01-2024
Public Assessment Report Public Assessment Report Slovak 25-03-2024
Patient Information leaflet Patient Information leaflet Slovenian 08-01-2024
Summary of Product characteristics Summary of Product characteristics Slovenian 08-01-2024
Public Assessment Report Public Assessment Report Slovenian 25-03-2024
Patient Information leaflet Patient Information leaflet Finnish 08-01-2024
Public Assessment Report Public Assessment Report Finnish 25-03-2024
Patient Information leaflet Patient Information leaflet Swedish 08-01-2024
Public Assessment Report Public Assessment Report Swedish 25-03-2024
Patient Information leaflet Patient Information leaflet Norwegian 08-01-2024
Summary of Product characteristics Summary of Product characteristics Norwegian 08-01-2024
Patient Information leaflet Patient Information leaflet Icelandic 08-01-2024
Summary of Product characteristics Summary of Product characteristics Icelandic 08-01-2024
Patient Information leaflet Patient Information leaflet Croatian 08-01-2024
Public Assessment Report Public Assessment Report Croatian 25-03-2024

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